chromosome deletion

Preferred Label : chromosome deletion;

MeSH definition : Actual loss of portion of a chromosome.;

MeSH synonym : deletions, chromosome; deletion, chromosome;

CISMeF synonym : chromosome deletions;

Wikipedia automatic translation : Deletion (genetics);

Related MeSH term : partial monosomy; Monosomies, Partial; Partial Monosomies; Monosomy, Partial;

MeSH annotation : coordinate IM with specific numbered chromosome or sex chromosome (IM) but not with CHROMOSOMES, HUMAN;

Wikipedia link : https://en.wikipedia.org/wiki/Deletion (genetics);

Details

Origin ID

D002872;

UMLS CUI

C0008628;

Automatic exact mappings (from CISMeF team)
- Y chromosome deletion [LOINC component]
- deletion [COVID-19 Thesaurus concept]
Currated CISMeF NLP mapping
- Chromosomal Deletion [NCIt concept]
- Chromosomal Loss [NCIt concept]
- Chromosomal deletion [MedDRA Preferred Term]
- Chromosomal deletion NOS [MedDRA LLT]
- Partial autosomal monosomy [ORDO Disease]
- Partial monosomy (morphologic abnormality) [SNOMED CT concept]
- chromosome deletion [Disease (Nov.)]
Record concept(s)
- chromosome deletion [MeSH concept]
- partial monosomy [MeSH concept]
Related MeSH Supplementary Concept(s)
- 10p deletion syndrome (Partial) [MeSH Supplementary Concept]
- 13q deletion syndrome [MeSH Supplementary Concept]
- 15q24 microdeletion [MeSH Supplementary Concept]
- 16p11.2 deletion syndrome [MeSH Supplementary Concept]
- 7p2 monosomy syndrome [MeSH Supplementary Concept]
- Chromosome 5q Deletion Syndrome [MeSH Supplementary Concept]
- Hypotonia-Cystinuria syndrome [MeSH Supplementary Concept]
- NF1 microdeletion syndrome [MeSH Supplementary Concept]
- Potocki-Shaffer syndrome [MeSH Supplementary Concept]
- Prader-Willi-Like syndrome associated with chromosome 6 [MeSH Supplementary Concept]
- X chromosome, monosomy Xp22 pter [MeSH Supplementary Concept]
- X chromosome, monosomy Xq28 [MeSH Supplementary Concept]
- chromosome 1, deletion q21 q25 [MeSH Supplementary Concept]
- chromosome 1, monosomy 1p [MeSH Supplementary Concept]
- chromosome 1, monosomy 1p22 p13 [MeSH Supplementary Concept]
- chromosome 1, monosomy 1p31 p22 [MeSH Supplementary Concept]
- chromosome 1, monosomy 1p32 [MeSH Supplementary Concept]
- chromosome 1, monosomy 1p34 p32 [MeSH Supplementary Concept]
- chromosome 1, monosomy 1q25 q32 [MeSH Supplementary Concept]
- chromosome 1, monosomy 1q32 q42 [MeSH Supplementary Concept]
- chromosome 1, monosomy 1q4 [MeSH Supplementary Concept]
- chromosome 10, monosomy 10q [MeSH Supplementary Concept]
- chromosome 10q23 deletion syndrome [MeSH Supplementary Concept]
- chromosome 10q26 deletion syndrome [MeSH Supplementary Concept]
- chromosome 11, deletion 11p [MeSH Supplementary Concept]
- chromosome 11p deletion syndrome [MeSH Supplementary Concept]
- chromosome 11p, partial deletion [MeSH Supplementary Concept]
- chromosome 11q partial deletion [MeSH Supplementary Concept]
- chromosome 12p deletion [MeSH Supplementary Concept]
- chromosome 12p partial deletion [MeSH Supplementary Concept]
- chromosome 14q, partial deletions [MeSH Supplementary Concept]
- chromosome 14q, terminal deletion [MeSH Supplementary Concept]
- chromosome 15q, partial deletion [MeSH Supplementary Concept]
- chromosome 15q13.3 microdeletion syndrome [MeSH Supplementary Concept]
- chromosome 17 deletion [MeSH Supplementary Concept]
- chromosome 17, deletion 17q23 q24 [MeSH Supplementary Concept]
- chromosome 17q21.31 deletion syndrome [MeSH Supplementary Concept]
- chromosome 18 deletion syndrome [MeSH Supplementary Concept]
- chromosome 18, deletion 18q23 [MeSH Supplementary Concept]
- chromosome 18p deletion syndrome [MeSH Supplementary Concept]
- chromosome 19q13.11 deletion syndrome [MeSH Supplementary Concept]
- chromosome 1p36 deletion syndrome [MeSH Supplementary Concept]
- chromosome 1q21.1 deletion syndrome, 1.35-Mb [MeSH Supplementary Concept]
- chromosome 1q21.1 duplication syndrome [MeSH Supplementary Concept]
- chromosome 1q43-Q44 deletion syndrome [MeSH Supplementary Concept]
- chromosome 2, monosomy 2p22 [MeSH Supplementary Concept]
- chromosome 2, monosomy 2pter p24 [MeSH Supplementary Concept]
- chromosome 2, monosomy 2q [MeSH Supplementary Concept]
- chromosome 2, monosomy 2q24 [MeSH Supplementary Concept]
- chromosome 20, deletion 20p [MeSH Supplementary Concept]
- chromosome 21, monosomy 21q22 [MeSH Supplementary Concept]
- chromosome 22, microdeletion 22 q11 [MeSH Supplementary Concept]
- chromosome 22q11.2 deletion syndrome, distal [MeSH Supplementary Concept]
- chromosome 2p16.1-P15 deletion syndrome [MeSH Supplementary Concept]
- chromosome 2q31.2 deletion syndrome [MeSH Supplementary Concept]
- chromosome 2q32-Q33 deletion syndrome [MeSH Supplementary Concept]
- chromosome 2q37 deletion syndrome [MeSH Supplementary Concept]
- chromosome 3, monosomy 3p [MeSH Supplementary Concept]
- chromosome 3, monosomy 3p14 p11 [MeSH Supplementary Concept]
- chromosome 3, monosomy 3p2 [MeSH Supplementary Concept]
- chromosome 3, monosomy 3p25 [MeSH Supplementary Concept]
- chromosome 3, monosomy 3q13 [MeSH Supplementary Concept]
- chromosome 3, monosomy 3q21 23 [MeSH Supplementary Concept]
- chromosome 3, monosomy 3q27 [MeSH Supplementary Concept]
- chromosome 3q29 deletion syndrome [MeSH Supplementary Concept]
- chromosome 4 short arm deletion [MeSH Supplementary Concept]
- chromosome 4, 4q terminal deletion syndrome [MeSH Supplementary Concept]
- chromosome 4, monosomy 4p14 p16 [MeSH Supplementary Concept]
- chromosome 4, monosomy 4q32 [MeSH Supplementary Concept]
- chromosome 4q- syndrome [MeSH Supplementary Concept]
- chromosome 6, deletion 6q13 q15 [MeSH Supplementary Concept]
- chromosome 6, monosomy 6p23 [MeSH Supplementary Concept]
- chromosome 6, monosomy 6q [MeSH Supplementary Concept]
- chromosome 6, monosomy 6q1 [MeSH Supplementary Concept]
- chromosome 6, monosomy 6q2 [MeSH Supplementary Concept]
- chromosome 6pter-P24 deletion syndrome [MeSH Supplementary Concept]
- chromosome 7, monosomy [MeSH Supplementary Concept]
- chromosome 7, monosomy 7q2 [MeSH Supplementary Concept]
- chromosome 7, monosomy 7q21 [MeSH Supplementary Concept]
- chromosome 7, monosomy 7q3 [MeSH Supplementary Concept]
- chromosome 8, monosomy 8p [MeSH Supplementary Concept]
- chromosome 8, monosomy 8p23 1 [MeSH Supplementary Concept]
- chromosome 8, monosomy 8q [MeSH Supplementary Concept]
- chromosome 8p deletion syndrome (partial) [MeSH Supplementary Concept]
- chromosome 9, partial monosomy 9p [MeSH Supplementary Concept]
- chromosome 9p deletion syndrome [MeSH Supplementary Concept]
- deafness, sensorineural, and male infertility [MeSH Supplementary Concept]
- deletion 13q syndrome, partial [MeSH Supplementary Concept]
- deletion 6q16 q21 [MeSH Supplementary Concept]
- fragile site 16p12 [MeSH Supplementary Concept]
- holoprosencephaly 10 [MeSH Supplementary Concept]
- homozygous 11p15-p14 deletion syndrome [MeSH Supplementary Concept]
- hypertrichosis terminalis, generalized, with or without gingival hyperplasia [MeSH Supplementary Concept]
- kleefstra syndrome [MeSH Supplementary Concept]
- male sterility due to Y-chromosome deletions [MeSH Supplementary Concept]
- monosomy 7 of bone marrow [MeSH Supplementary Concept]
- otodental dysplasia [MeSH Supplementary Concept]
- telomeric 22q13 monosomy syndrome [MeSH Supplementary Concept]
See also
- gene deletion [MeSH Descriptor]
See also (suggested by CISMeF)
- 22q11 deletion syndrome [MeSH Descriptor]
- cri-du-chat syndrome [MeSH Descriptor]
- wolf-hirschhorn syndrome [MeSH Descriptor]
See also inter- (CISMeF)
- Chromosome Y deletion [ICD-11 More detail]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- Chromosomal Deletion [NCIt concept]
- Chromosomal deletion [MedDRA Preferred Term]
- Chromosomal deletion NOS [MedDRA LLT]
- chromosome deletion [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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